Experiments
Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).
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SMART: spatial multi-omic aggregation using graph neural networks and metric learning.
PMID 41896208 · PMC13031631 · Nature communications · 2026 · 8 claims · 5 setups
SMART accurately identifies spatial regions of anatomical structures and is compatible with spatial datasets of any type and number of omics layers
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STAN, a computational framework for inferring spatially informed transcription factor activity.
PMID 41521668 · PMC12784991 · Nucleic acids research · 2026 · 7 claims · 7 setups
STAN, a linear mixed-effects (spatially weighted regression) model, integrates TF-target gene priors, gene expression, spatial coordinates, and histological image features to predict spot-specific TF activity in spatial transcriptomics data
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Spatial transcriptomics unveils immune cellular ecosystems associated with patient survival in diffuse large B-cell lymphoma.
PMID 42010788 · PMC13102037 · Oncoimmunology · 2026 · 7 claims · 7 setups
DLBCL tissues are organized into six recurrent, spatially defined cellular ecosystems (Cell-Eco) with distinct immune compositions, transcriptional programs, and neighborhood architectures.
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Single-cell spatial transcriptomics reveals tumor microenvironment heterogeneity in primary and lymph node-metastatic small cell lung cancer.
PMID 41916294 · PMC13130650 · Cell reports. Medicine · 2026 · 8 claims · 8 setups
Three malignant subclusters (C5, C6, C9) are enriched in LNM tumors and display distinct metabolic and angiogenic programs alongside spatial immune exclusion
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SpaNiche: spatial niche analysis to explore colocalization patterns and cellular interactions in spatial transcriptomics data.
PMID 42015285 · PMC13231777 · Genome biology · 2026 · 8 claims · 6 setups
SpaNiche integrates smoothed cell-type abundance and ligand-receptor expression matrices via graph-regularized joint NMF, across multiple spatial views, to identify colocalization patterns
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ISG15-driven immune modulation and tumor progression in breast cancer metastasis: insights from single-cell and spatial transcriptomics.
PMID 41639695 · PMC12958617 · BMC medicine · 2026 · 8 claims · 8 setups
CSC proportion is elevated in lymph node metastatic tumor tissue (BRCA_LNMT) compared to primary tumor (BRCA_PT)
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Spatiotemporal Transcriptomics Characterizes Immune Microenvironment During Mouse Liver Aging.
PMID 42010880 · PMC13096584 · Aging cell · 2026 · 8 claims · 8 setups
T cells are the immune cell population with the most pronounced transcriptomic alterations during liver aging
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Secreted phospholipase PLA2G5 acts as a hemolytic factor in sepsis.
PMID 42065235 · PMC13132393 · The Journal of clinical investigation · 2026 · 8 claims · 8 setups
Pla2g5 gene expression is induced in the colon and small intestine during LPS-induced endotoxemia and CLP-induced sepsis in mice
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Single-cell and spatial profiling highlights TB-induced myofibroblasts as drivers of lung pathology.
PMID 41489684 · PMC12767585 · The Journal of experimental medicine · 2026 · 8 claims · 8 setups
MMP1+CXCL5+ fibroblasts and SPP1+ macrophages are linked to TB disease and TB lung granuloma and reveal targetable cellular cross talk underlying TB immunopathology
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Identification of cycling regulatory T cell precursors as conductors of immune escape during breast carcinoma progression.
PMID 41997138 · PMC13213619 · Cancer cell · 2026 · 8 claims · 8 setups
A novel proliferative Treg precursor state, cycling Treg (cycTreg: FOXP3^int, MKI67^hi, IKZF2/4^int-hi), is absent in normal breast, low in DCIS, and strongly expanded in IBC
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Reprogramming of stroma-derived chemokine networks drives the loss of tissue organization in nodal B cell lymphoma.
PMID 41882179 · PMC13035477 · Nature cancer · 2026 · 8 claims · 8 setups
LN-resident stromal cells (FRCs, BECs, LECs) drive chemokine-based lymphocyte zonation, and disruption of this system underlies the loss of tissue organization in nodal B cell lymphoma